Stevenson W G, Sager P, Nademanee K, Hassan H, Middlekauff H R, Saxon L A, Wiener I
Division of Cardiology, UCLA School of Medicine.
Herz. 1992 Jun;17(3):158-70.
The approach to localizing sites for catheter ablation of ventricular tachycardia foci depends on the type of tachycardia. In large reentry circuits such as those arising from infarct scars, areas of slow conduction in and around the scar should be targeted. During sinus rhythm, these can be suspected from the presence of fractionated electrograms and, at some sites, long stimulus to QRS delays during pacing. Slow conduction areas can be classified as: 1. central slow conduction zone sites, 2. exits from the slow conduction zone, 3. entrances to the slow conduction zone, and 4. bystander areas which are not involved in the tachycardia circuit. In the central slow conduction zone stimulation entrains or resets tachycardia with a long stimulus to QRS (S-QRS) delay (40 to greater than 300 ms) without altering the QRS morphology (entrainment with concealed fusion). At slow conduction zone exits, presystolic electrograms are recorded during VT, the pacemap matches the VT QRS morphology, and with pacing during VT the S-QRS interval is relatively short and VT may or may not be entrained. At entrances to the slow conduction zone electrogram timing is variable but early diastolic electrograms are expected and the pace-map QRS may differ from the VT QRS morphology. Relatively late stimuli or slow trains of stimuli entrain VT with concealed fusion with a relatively longer S-QRS interval than observed in the central slow conduction zone. Early stimuli may entrain VT while altering the QRS morphology due to propagation of the stimulated antidromic wavefront out of the scar from a site other than the tachycardia exit. At bystander sites electrogram timing, pace-mapping, and the effects of programmed stimulation are variable but may occasionally mimic reentry circuit sites. Relatively late stimuli are likely to capture the site without altering the VT. If discrete electrograms are present, analysis of these during pacing may provide further evidence that the site is not in the reentry circuit. Catheter ablation will probably be most effective at central slow conduction zone sites. When VT originates from a small focus surrounded by normal myocardium, such as is likely for idiopathic RV outflow tract and some idiopathic left ventricular tachycardias, presystolic electrical activity and pacemapping are likely to identify the tachycardia focus. For macroreentry involving the bundle branches, the right bundle branch can be easily targeted.
对于室性心动过速病灶进行导管消融的部位定位方法取决于心动过速的类型。在诸如由梗死瘢痕引起的大折返环路中,应将瘢痕内及周围的缓慢传导区域作为靶点。在窦性心律期间,可根据碎裂电图的存在以及在某些部位起搏时刺激至QRS波的延迟时间较长来怀疑这些区域。缓慢传导区域可分为:1. 中央缓慢传导区部位;2. 缓慢传导区的出口;3. 缓慢传导区的入口;4. 未参与心动过速环路的旁观者区域。在中央缓慢传导区进行刺激时,可通过较长的刺激至QRS波(S-QRS)延迟(40至大于300毫秒)来拖带或重置心动过速,且不改变QRS波形态(隐匿性融合拖带)。在缓慢传导区出口处,室性心动过速期间可记录到收缩前电图,起搏标测与室性心动过速的QRS波形态匹配,并且在室性心动过速期间进行起搏时,S-QRS间期相对较短,室性心动过速可能被拖带也可能不被拖带。在缓慢传导区入口处,电图的时间变化不定,但预期会出现舒张早期电图,起搏标测的QRS波可能与室性心动过速的QRS波形态不同。相对较晚的刺激或缓慢的刺激序列可通过隐匿性融合拖带室性心动过速,其S-QRS间期比在中央缓慢传导区观察到的要长。早期刺激可能会拖带室性心动过速,同时由于刺激的逆向波前从除心动过速出口外的部位传出瘢痕而改变QRS波形态。在旁观者部位,电图时间、起搏标测以及程控刺激的效果变化不定,但偶尔可能会模仿折返环路部位。相对较晚的刺激可能会夺获该部位而不改变室性心动过速。如果存在离散电图,起搏期间对其进行分析可能会提供进一步证据表明该部位不在折返环路中。导管消融可能在中央缓慢传导区部位最为有效。当室性心动过速起源于被正常心肌包围的小病灶时,如特发性右心室流出道和一些特发性左心室心动过速可能出现的情况,收缩前电活动和起搏标测可能会确定心动过速病灶。对于涉及束支的大折返,右束支很容易成为靶点。